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Wilate FDA Approval History

FDA Approved: Yes (First approved December 4, 2009)
Brand name: Wilate
Generic name: von Willebrand Factor/Coagulation Factor VIII Complex (Human)
Dosage form: Injection
Company: Octapharma USA
Treatment for: von Willebrand Disease, Hemophilia A

Wilate (von Willebrand Factor/Coagulation Factor VIII Complex (Human)) is used in the management of von Willebrand disease and hemophilia A.

Development timeline for Wilate

DateArticle
Dec  7, 2023Approval FDA Grants Expanded Approval to Wilate as the First VWF Concentrate for Prophylaxis in All Types of VWD
Oct  8, 2019Approval FDA Approves Octapharma’s Wilate® for Hemophilia A in Adult and Adolescent Patients
Aug 13, 2015Approval FDA Approves Wilate License Supplement - Perioperative Management of Bleeding in Patients with von Willebrand Disease
Dec  8, 2009Approval Octapharma USA Announces FDA Approval of Wilate - the First Replacement Therapy Developed Specifically for von Willebrand Disease

Further information

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